8-Chloro-6-(chloromethyl)-2-methylocta-1,6-dien-3-ol

Details

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Internal ID 31218b04-2236-4c2f-bf5c-ded6ed2459a4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 8-chloro-6-(chloromethyl)-2-methylocta-1,6-dien-3-ol
SMILES (Canonical) CC(=C)C(CCC(=CCCl)CCl)O
SMILES (Isomeric) CC(=C)C(CCC(=CCCl)CCl)O
InChI InChI=1S/C10H16Cl2O/c1-8(2)10(13)4-3-9(7-12)5-6-11/h5,10,13H,1,3-4,6-7H2,2H3
InChI Key ZYGUWNRHQQMKCV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16Cl2O
Molecular Weight 223.14 g/mol
Exact Mass 222.0578205 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Chloro-6-(chloromethyl)-2-methylocta-1,6-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.5398 53.98%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4831 48.31%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9242 92.42%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8553 85.53%
P-glycoprotein inhibitior - 0.9722 97.22%
P-glycoprotein substrate - 0.8275 82.75%
CYP3A4 substrate - 0.5359 53.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7218 72.18%
CYP3A4 inhibition - 0.8669 86.69%
CYP2C9 inhibition - 0.8831 88.31%
CYP2C19 inhibition - 0.8254 82.54%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition - 0.7145 71.45%
CYP2C8 inhibition - 0.9636 96.36%
CYP inhibitory promiscuity - 0.8990 89.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5713 57.13%
Carcinogenicity (trinary) Non-required 0.5573 55.73%
Eye corrosion + 0.5561 55.61%
Eye irritation - 0.6772 67.72%
Skin irritation + 0.5891 58.91%
Skin corrosion - 0.7277 72.77%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5997 59.97%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.7628 76.28%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8100 81.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7432 74.32%
Acute Oral Toxicity (c) III 0.5368 53.68%
Estrogen receptor binding - 0.8415 84.15%
Androgen receptor binding - 0.9180 91.80%
Thyroid receptor binding - 0.8056 80.56%
Glucocorticoid receptor binding + 0.5724 57.24%
Aromatase binding - 0.8742 87.42%
PPAR gamma - 0.5869 58.69%
Honey bee toxicity - 0.7549 75.49%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8462 84.62%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.57% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.46% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.00% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 84.62% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.92% 97.25%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.81% 92.29%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.71% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.23% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72732360
LOTUS LTS0267526
wikiData Q105386136